@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_head
{
this:
np:hasAssertion
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion
;
np:hasProvenance
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_provenance
;
np:hasPublicationInfo
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion
a
np:Assertion
.
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_provenance
a
np:Provenance
.
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion
{
miriam-gene:3858
a
ncit:C16612
.
lld:C0037277
a
ncit:C7057
.
dgn-gda:DGN1a0ed7a311b5142ab697256223b98492
sio:SIO_000628
miriam-gene:3858
,
lld:C0037277
;
a
sio:SIO_001121
.
}
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_provenance
{
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_assertion
dcterms:description
"[Epidermolytic palmoplantar keratoderma (EPPK) is an autosomal dominant genodermatosis characterized by epidermolytic hyperkeratosis strictly confined to the palms and soles, and usually associated with mutations in the keratin K9 gene (KRT9).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15214894
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP158069.RA4bFTcMg-tT4BG0DwFRQwqqMU-19EI9dU36LFWr3t1gk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:25+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}